Mindray DP-8500 User manual

DP-8500/DP-8300
Digital Ultrasonic Diagnostic
Imaging System
Operator’s Manual
[Basic Volume]

Contents
Intellectual Property Statement .......................................................................................................... I
Responsibility on the Manufacturer Party .......................................................................................... I
Warranty ............................................................................................................................................ II
Definitions..................................................................................................................................... II
Exemptions................................................................................................................................... II
Return Policy .................................................................................................................................... III
Return Procedure........................................................................................................................ III
Company Contact........................................................................................................................ III
Important Information ....................................................................................................................... IV
About This Manual ...........................................................................................................................IV
Notation Conventions .......................................................................................................................IV
Operator’s Manuals...........................................................................................................................V
Manuals on Paper .............................................................................................................................V
Software Interfaces in this Manual .................................................................................................... V
Conventions ......................................................................................................................................V
Safety Precautions .............................................................................................................. VI
Meaning of Signal Words .................................................................................................................VI
Meaning of Safety Symbols..............................................................................................................VI
Safety Precautions ...........................................................................................................................VI
Latex Alert .........................................................................................................................................X
Warning Labels.................................................................................................................................XI
1Overview...................................................................................................................... 1-1
1.1 General................................................................................................................................. 1-1
1.2 Product Specifications.......................................................................................................... 1-1
1.2.1 Environmental Conditions............................................................................................. 1-1
1.2.2 Dimensions and Weight................................................................................................ 1-1
1.3 System Configuration........................................................................................................... 1-2
1.3.1 Standard Configuration................................................................................................. 1-2
1.3.2 Transducers Available .................................................................................................. 1-2
1.3.3 Optional Parts ............................................................................................................... 1-3
1.3.4 Peripherals Supported.................................................................................................. 1-3
1.4 System Introduction.............................................................................................................. 1-3
1.4.1 Introduction of Each Unit .............................................................................................. 1-4
1.4.2 I/O Panel....................................................................................................................... 1-5
1.4.3 Control Panel ................................................................................................................ 1-6
1.4.4 Symbols ........................................................................................................................ 1-8
Contents i

2Preparing the System ................................................................................................. 2-1
2.1 Setup and Connections ........................................................................................................2-1
2.1.1 Moving and Placing the System ...................................................................................2-1
2.1.2 Connecting the Power Cord..........................................................................................2-1
2.1.3 Connecting/Disconnecting the Transducers .................................................................2-2
2.1.4 Connecting/Disconnecting USB device ........................................................................2-3
2.1.5 Connecting a Footswitch............................................................................................... 2-3
2.1.6 Connecting a Printer .....................................................................................................2-3
2.1.7 Connecting an External Display....................................................................................2-4
2.2 Powering ON/OFF ................................................................................................................2-4
2.2.1 Checking before Powering ON .....................................................................................2-4
2.2.2 Powering ON.................................................................................................................2-5
2.2.3 Restarting......................................................................................................................2-5
2.2.4 Powering OFF...............................................................................................................2-6
2.3 Main Interface.......................................................................................................................2-6
2.4 Basic Operations ..................................................................................................................2-7
3Beginning an Exam..................................................................................................... 3-1
3.1 Entering Patient Information.................................................................................................3-1
3.2 Get Patient Information ........................................................................................................3-2
3.2.1 iStation ..........................................................................................................................3-2
3.2.2 Work List .......................................................................................................................3-3
3.3 Selecting the Exam Mode ....................................................................................................3-3
3.4 Selecting the Image Mode....................................................................................................3-3
3.5 Adjusting the Image..............................................................................................................3-4
3.5.1 Zooming ........................................................................................................................3-4
3.5.2 Zooming with Thumbnail...............................................................................................3-4
3.5.3 Rotating and Flipping the Image...................................................................................3-5
3.5.4 Image Merge.................................................................................................................3-5
3.6 Cine Review .........................................................................................................................3-5
3.6.1 Cine Review of B Mode ................................................................................................3-6
3.6.2 Cine Review of 2B/4B Mode.........................................................................................3-7
3.6.3 Cine Review of M/M+B Mode .......................................................................................3-7
3.7 Brief Introductions to Measurement .....................................................................................3-7
3.7.1 Basic Operations and Buttons ......................................................................................3-7
3.7.2 Measurement Items ...................................................................................................... 3-8
4Optimizing the Image.................................................................................................. 4-1
4.1 Basic Operations ..................................................................................................................4-1
4.2 B Mode .................................................................................................................................4-2
4.2.1 Depth ............................................................................................................................4-2
ii Contents

4.2.2 Frequency..................................................................................................................... 4-2
4.2.3 Gain .............................................................................................................................. 4-3
4.2.4 Acoustic Power ............................................................................................................. 4-3
4.2.5 TGC .............................................................................................................................. 4-4
4.2.6 Focus ............................................................................................................................ 4-4
4.2.7 B/M Dyn Rng (Dynamic Range) ................................................................................... 4-5
4.2.8 Img Enhance (Image Enhance).................................................................................... 4-5
4.2.9 Frame Avg (Frame Average) ........................................................................................ 4-5
4.2.10 TSI ................................................................................................................................ 4-6
4.2.11 Scan Mode.................................................................................................................... 4-6
4.2.12 IP................................................................................................................................... 4-7
4.2.13 B/M Post Process ......................................................................................................... 4-7
4.3 M Mode ................................................................................................................................ 4-8
4.3.1 M Speed........................................................................................................................ 4-8
4.3.2 Edge Enhance .............................................................................................................. 4-9
4.3.3 M Soften ....................................................................................................................... 4-9
5Annotating the Image ................................................................................................. 5-1
5.1 Comments ............................................................................................................................ 5-1
5.1.1 Adding Comments ........................................................................................................ 5-1
5.1.2 Adding Arrow ................................................................................................................ 5-2
5.1.3 Moving Comments/Arrows............................................................................................ 5-2
5.1.4 Editing Comments ........................................................................................................ 5-2
5.1.5 Deleting Comments/Arrows.......................................................................................... 5-2
5.2 Body Mark ............................................................................................................................ 5-2
5.2.1 Adding Body Mark ........................................................................................................ 5-3
5.2.2 Moving the Body Mark.................................................................................................. 5-3
5.2.3 Editing the Body Mark .................................................................................................. 5-3
5.2.4 Deleting the Body Mark ................................................................................................ 5-3
6Auxiliary Functions .................................................................................................... 6-1
6.1 Biopsy Guide ........................................................................................................................ 6-1
6.1.1 Basic Operations .......................................................................................................... 6-1
6.1.2 Adjusting the Guide Line .............................................................................................. 6-1
6.2 Lithotrity................................................................................................................................ 6-2
7File Management......................................................................................................... 7-1
7.1 Formats of Files.................................................................................................................... 7-1
7.2 Saving Files.......................................................................................................................... 7-1
7.3 File Management.................................................................................................................. 7-1
7.4 Backup ................................................................................................................................. 7-2
Contents iii

7.4.1 Backup of Data .............................................................................................................7-2
7.4.2 Erasing Optical Disc......................................................................................................7-3
7.5 iVision ...................................................................................................................................7-3
8Preset ...........................................................................................................................8-1
8.1 Basic Operations ..................................................................................................................8-2
8.2 System Preset ......................................................................................................................8-2
8.2.1 Region...........................................................................................................................8-2
8.2.2 General .........................................................................................................................8-3
8.2.3 Image Preset.................................................................................................................8-3
8.2.4 Meas Param..................................................................................................................8-4
8.2.5 OB.................................................................................................................................8-5
8.2.6 Key Config ....................................................................................................................8-5
8.2.7 Option ...........................................................................................................................8-6
8.3 Exam Preset .........................................................................................................................8-6
8.3.1 Exam Selection .............................................................................................................8-6
8.3.2 Exam Config .................................................................................................................8-7
8.4 Image Preset ........................................................................................................................8-7
8.5 Measure Preset ....................................................................................................................8-9
8.5.1 Measure ........................................................................................................................8-9
8.6 Comment Preset.................................................................................................................8-10
8.6.1 Comment Library ........................................................................................................ 8-11
8.7 DICOM................................................................................................................................8-15
8.8 Manage Settings.................................................................................................................8-16
8.9 Maintenance .......................................................................................................................8-17
9Cleaning and Maintaining the System.......................................................................9-1
9.1 Daily Maintenance ................................................................................................................9-1
9.1.1 Cleaning the System.....................................................................................................9-1
9.1.2 Backup of Data .............................................................................................................9-2
9.2 Maintenance Checks by Service Engineer ..........................................................................9-2
9.3 Consumables and Periodic Part Replacement ....................................................................9-2
9.4 Troubleshooting....................................................................................................................9-2
10 Acoustic Output ........................................................................................................ 10-1
10.1 Concerns with Bioeffects ....................................................................................................10-1
10.2 Prudent Use Statement ......................................................................................................10-1
10.3 ALARA Principle (As Low As Reasonably Achievable) ......................................................10-1
10.4 Derated Ultrasonic Output Parameters ..............................................................................10-2
10.5 Measurement Uncertainty ..................................................................................................10-2
10.6 Parameters Affecting Acoustic Power ................................................................................10-2
iv Contents

Contents v
10.7 Acoustic Power Setting ...................................................................................................... 10-3
10.8 Operations That Change Acoustic Output Power .............................................................. 10-3
10.9 References for Acoustic Power and Safety........................................................................ 10-4
Appendix A Transducer Maximum Surface Temperature .......................................A-1
Appendix B Accuracy of Measurement ....................................................................B-1
Appendix C Safety Classification ..............................................................................C-1
Appendix D Guidance and Declaration.....................................................................D-1

© 2009 Shenzhen Mindray Bio-Medical Electronics Co., Ltd. All rights Reserved.
For this Operator’s Manual, the issue date is 2009-05.
Intellectual Property Statement
SHENZHEN MINDRAY BIO-MEDICAL ELECTRONICS CO., LTD. (hereinafter called Mindray)
owns the intellectual property rights to this Mindray product and this manual. This manual may
refer to information protected by copyright or patents and does not convey any license under the
patent rights or copyright of Mindray, or of others.
Mindray intends to maintain the contents of this manual as confidential information. Disclosure of
the information in this manual in any manner whatsoever without the written permission of Mindray
is strictly forbidden.
Release, amendment, reproduction, distribution, rental, adaptation, translation or any other
derivative work of this manual in any manner whatsoever without the written permission of Mindray
is strictly forbidden.
, , , , BeneView, WATO, BeneHeart,
are the trademarks, registered or otherwise, of Mindray in China and other countries. All oth
trademarks that appear in this manual are used only for informational or editorial purposes. They
are the property of their respective owners.
er
Responsibility on the Manufacturer Party
Contents of this manual are subject to change without prior notice.
All information contained in this manual is believed to be correct. Mindray shall not be liable for
errors contained herein or for incidental or consequential damages in connection with the
furnishing, performance, or use of this manual.
Mindray is responsible for the effects on safety, reliability and performance of this product, only if:
zall installation operations, expansions, changes, modifications and repairs of this product
are conducted by Mindray authorized personnel;
zthe electrical installation of the relevant room complies with the applicable national and
local requirements; and
zthe product is used in accordance with the instructions for use.
Note
This equipment must be operated by skilled/trained clinical professionals.
Warning
It is important for the hospital or organization that employs this equipment to carry out a
reasonable service/maintenance plan. Neglect of this may result in machine breakdown or
personal injury.
Intellectual Property Statement I

Warranty
THIS WARRANTY IS EXCLUSIVE AND IS IN LIEU OF ALL OTHER WARRANTIES, EXPRESSED
OR IMPLIED, INCLUDING WARRANTIES OF MERCHANTABILITY OR FITNESS FOR ANY
PARTICULAR PURPOSE.
Definitions
zMain unit: Integrated facilities which implements the specified function separately.
Generally speaking, the main unit should include power supply, control system and some
functional modules.
zAccessories: Materials connected to the main unit to extend or implement specified
function.
zConsumables: Disposable or short-life parts which should be replaced each time after
use or periodically.
Exemptions
Mindray's obligation or liability under this warranty does not include any transportation or other
charges or liability for direct, indirect or consequential damages or delay resulting from the
improper use or application of the product or the use of parts or accessories not approved by
Mindray or repairs by people other than Mindray authorized personnel.
This warranty shall not extend to:
Malfunction or damage caused by improper use or man-made failure.
Malfunction or damage caused by unstable or out-of-range power input.
Malfunction or damage caused by force majeure such as fire and earthquake.
Malfunction or damage caused by improper operation or repair by unqualified or
unauthorized service people.
Malfunction of the instrument or part whose serial number is not legible enough.
Others not caused by instrument or part itself.
The standard warranty period is as below:
Main unit: 18 months from shipment
Accessories: 15 months from shipment
Main Accessories include transducers, cables, gel bottle and transducer holders
Consumables: N/A
II Warranty

Return Policy
Return Procedure
In the event that it becomes necessary to return this product or part of this product to Mindray, the
following procedure should be followed:
1. Return authorization: Contact the international Customer Service Department and obtain a
Return Materials Authorization number. This number must appear on the outside of the
shipping container. Returned shipments will not be accepted if the number is not clearly visible.
Please provide the model number, serial number, and a brief description of the reason for
return.
2. Freight policy: The customer is responsible for freight charges when this product is shipped to
Mindray for service (this includes customs charges).
3. Return address: Please send the part(s) or equipment to the address offered by the
international Customer Service Department.
Company Contact
Manufacturer: Shenzhen Mindray Bio-medical Electronics Co., Ltd.
E-mail Address: [e-mail]
Tel: [phone] 26582888
Fax: [phone] 26582500
EC-Representative: Shanghai International Holding Corp. GmbH(Europe)
Address: Eiffestraβe 80, Hamburg 20537, Germany
Tel: [phone]
Fax: [phone]
Return Policy III

Important Information
1. It is the customer’s responsibility to maintain and manage the system after delivery.
2. The warranty does not cover the following items, even during the warranty period:
(1) Damage or loss due to misuse or abuse.
(2) Damage or loss caused by Acts of God such as fires, earthquakes, floods, lightning, etc.
(3) Damage or loss caused by failure to meet the specified conditions for this system, such as
inadequate power supply, improper installation or environmental conditions.
(4) Damage or loss due to use of the system outside the region where the system was
originally sold.
(5) Damage or loss involving the system purchased from a source other than Mindray or its
authorized agents.
3. This system shall not be used by persons other than fully qualified and certified medical
personnel.
4. Do not make changes or modifications to the software or hardware of this system.
5. In no event shall Mindray be liable for problems, damage, or loss caused by relocation,
modification, or repair performed by personnel other than those designated by Mindray.
6. The purpose of this system is to provide physicians with data for clinical diagnosis.
7. It is the physician’s responsibility for diagnostic procedures. Mindray shall not be liable for the
results of diagnostic procedures.
8. Important data must be backed up on external memory media.
9. Mindray shall not be liable for loss of data stored in the memory of this system caused by
operator error or accidents.
10. This manual contains warnings regarding foreseeable potential dangers, but you shall always
be alert to dangers other than those indicated as well. Mindray shall not be liable for damage
or loss that results from negligence or from ignoring the precautions and operating instructions
described in this operator’s manual.
11. If the manager for this system is changed, be sure to hand over this operator’s manual to the
new manager.
About This Manual
This operator’s manual describes the operating procedures for digital ultrasonic diagnostic imaging
system DP-8500/DP-8300. To ensure safe and correct operations, carefully read and understand
the manual before operating the system.
Notation Conventions
In this operator’s manual, the following words are used besides the safety precautions (refer to
"Safety Precautions"). Please read this operator’s manual before using the system.
CAUTION: The digital ultrasonic diagnostic imaging system is not intended for
ophthalmic use. Its use in this clinical specialty is contraindicated.
IV Important Information

Operator’s Manuals
The operator’s manuals consist of manuals for the main unit and manuals for transducers. The
English manuals are provided on paper; however, the manuals, which are translated into
languages other than English, are provided in CD (Compact Disc).
The content of the operator manual, such as screens, menus or descriptions, may be different from
what you see in your system. The content varies depending upon the software version, options
and configuration of the system.
Manuals on Paper
zOperator’s Manual [Basic Volume]: Describes the basic functions and operations of the
system, safety precautions, exam modes, imaging modes, preset, maintenance and
acoustic output, etc.
zOperator’s Manual [Advanced Volume]: Describes measurement preset, measurements
and calculations, etc.
zOperator’s Manual [Acoustic Power Data and Surface Temperature Data]: Contains data
tables of acoustic output for transducers.
zOperation Note: Contains quick guide for basic operations of the system.
zOperator’s Manuals of Transducers: Describe the operation, cleaning, disinfection and
sterilization procedures for transducers.
Software Interfaces in this Manual
Depending on the software version, preset settings and optional configuration, the actual
interfaces may be different from those in this manual.
Conventions
In this manual, these conventions are used to describe the buttons on the control panel, the items
in menu, buttons in dialog box and some basic operations:
z<Buttons>: The angular bracket indicates buttons on control panel.
z[Items in menu and buttons in dialog box]: The square bracket indicates items in menu or
buttons in dialog box.
zClick [Items or Button]: Move the cursor to the item or button and press <Set>.
z[Items in Menu]Æ[Items in Submenu]: Selects a submenu item following the path.
z[Dyn Rng (Value)]: Indicates menu items with parameter, (value) shows the current value
of the item.
z<Multifunctional Knob (R)> and <Multifunctional Knob (L)>: Indicate the right and left
multifunctional knobs.
Operator’s Manuals V

Safety Precautions
Meaning of Signal Words
In this operator’s manual, the signal words DANGER, WARNING, CAUTION
and NOTE are used regarding safety and other important instructions. The signal words and their
meanings are defined as follows. Please understand their meaning before reading this manual.
Signal words Meaning
DANGER Indicates an imminently hazardous situation that, if not avoided, will
result in death or serious injury.
WARNING Indicates a potentially hazardous situation that, if not avoided, could
result in death or serious injury.
CAUTION Indicates a potentially hazardous situation that, if not avoided, may
result in minor or moderate injury.
NOTE Indicates a potentially hazardous situation that, if not avoided, may result in
property damage.
Meaning of Safety Symbols
Symbols Description
Type-BF applied part
The ultrasound transducers connected to this system are Type-BF applied parts.
"Attention" indicates the points that you should pay attention to. Be sure to read
the operator’s manual concerning these points before using the system.
Safety Precautions
Please observe the following precautions to ensure patient’s and operator’s safety when using this
system.
DANGER: Do not use flammable gasses, such as anesthetic gas or hydrogen, or
flammable liquids such as ethanol, near this system, because there is
danger of explosion.
WARNING: 1. Connect the adapter power plug of this system and power plugs of
the peripherals to wall receptacles that meet the ratings indicated
on the rating nameplate. Using a multifunctional receptacle may
affect the system grounding performance, and cause the leakage
current to exceed safety requirements.
You must use the power adapter provided with the system;
otherwise electric shock may result.
VI Meaning of Signal Words

WARNING: 2. Use the printing cable provided with this system to connect the
printer. Electric shock may result.
3. Before cleaning the system, disconnect the power cord from the
outlet. System failure and electric shock may result.
4. Use the transducer carefully. In case that the body contacts the
scratched transducer surface, immediately stop using the
transducer and contact the Mindray sales office, customer service
department or representative. There is risk of electric shock if
using the scratched transducer.
5. This system is not water-proof. Do not use this system in any
place where water leakage may occur. If any water is sprayed on or
into the system, electric shock may result. If water is accidentally
sprayed on or into the system, contact Mindray Customer Service
Department or sales representative.
6. Do not allow the patient to contact the live parts of the digital
ultrasonic diagnostic imaging system or other devices, e.g. signal
I/O ports. Electric shock may occur.
7. Do not use an aftermarket transducer other than those specified
by Mindray. The transducers may damage the system causing a
profound failure, e.g. a fire in the worst case.
8. Do not subject the transducers to knocks or drops. Use of a
defective transducer may cause an electric shock.
9. Do not open the shell or front panel. If open the shell when the
machine is powered on, there may be a short circuit or electric
shock.
10. Do not use this system at the same time with other equipment
such as electric knife, high-frequency therapy equipment and
defibrillator, etc., Otherwise there is a danger of electric shock.
11. Accessory equipment connected to the analog and digital
interfaces must comply with the relevant IEC standards (e.g., IEC
60950 information technology equipment safety standard and IEC
60601-1 medical equipment standard). Furthermore all
configurations must comply with the standard IEC60601-1-1. It is
the responsibility of the person, who connects additional
equipment to the signal input or output ports and configures a
medical system, to verify that the system complies with the
requirements of IEC60601-1-1. If you have any questions regarding
these requirements, consult your sales representative.
12. Prolonged and repeated use of keyboards may result in hand or
arm nerve disorders for some individuals. Observe the local safety
or health regulations concerning the use of keyboards.
Safety Precautions VII

CAUTION: 1. Precautions concerning clinical examination techniques:
(1) This system must be used only by qualified medical professionals.
(2) This operator’s manual does not describe clinical examination
techniques. The clinician should select the proper examination
techniques based on specialized training and clinical experience.
2. Malfunctions due to radio wave:
(1) If a radio wave emitting device is used in the proximity of this
system, it may interfere with operations. Do not bring or use devices
that generate radio waves, such as cellular telephones,
transceivers, and radio controlled toys, in the room where the
system is installed.
(2) If a person brings a device that generates radio waves near the
system, ask him / her to immediately turn OFF the device.
3. Precautions concerning movement of the system:
(1) Object placed on the monitor may fall and injure an individual.
(2) Fasten and fully secure any peripheral device before moving the
system. A loose peripheral device may fall and injure an individual.
(3) Do not expose the system to excessive vibration through
transportation. Mechanical damage may result.
(4) Always keep the system dry. Avoid transporting this system quickly
from a cold place to a warm place; otherwise condensation or water
droplets may form allowing a short circuit and possible electric
shock.
4. If the circuit protector is tripped, it indicates that the system or a
peripheral device was improperly shut down and the system is unstable.
You cannot repair the system under this circumstance and must call the
Mindray Customer Service Department or sales representative.
5. There is no risk of high-temperature burns during routine ultrasound
examinations. It is possible for the surface temperature of the
transducer to exceed the body temperature of a patient due to
environmental temperature and exam type combinations. If a patient
complains of any excessive heat from the transducer, immediately stop
scanning. To prevent patient burns, ensure there is no surface damage
to the transducer. Do not apply the transducer to the same region on
the patient for a long time. Apply the transducer only for a period of time
required for the purpose of diagnosis.
6. Do not use the system to examine a fetus for a long period of time.
7. The system and its accessories are not disinfected or sterilized prior to
delivery. The operator is responsible for the cleaning and disinfection of
transducers and sterilization of biopsy brackets according to the
manuals, prior to the use. All items must be thoroughly processed to
completely remove harmful residual chemicals or gasses that are
harmful to the human body or that may damage the accessory.
8. It is necessary to press <Patient> to end the current scan that is in
progress and clear the current Patient Information field. Otherwise new
patient data may be combined with the previous patient data.
9. Do not connect or disconnect the system’s power cord or its accessories
(e.g., a printer) without turning OFF the power first. This may damage
the system and its accessories or cause electric shock.
10. Before using the digital ultrasonic diagnostic imaging system to perform
an exam, please carefully read “10 Acoustic Output”.
VIII Safety Precautions

CAUTION: 11. The cover contains natural rubber latex and talc that can cause allergic
reactions in some individuals.
12. Please use the ultrasound gel compliant with the relevant local
regulations.
13. Do not connect this system to outlets with the same circuit breakers and
fuses that control the current of devices such as life-support systems. If
this system malfunctions and generates overcurrent, or when there is an
instantaneous current at power ON, the circuit breakers and fuses of the
building’s supply circuit may be tripped.
NOTE: 1. Do not use the system in the vicinity of strong electromagnetic field (such as a
transformer), which may affect the performance of the system.
2. Do not use the system in the vicinity of high-frequency radiation source, which may
affect the performance of the system or even lead to failure.
3. When using or placing the system, keep the system horizontal to avoid disbalance.
4. To avoid damaging the system, do not use it in following environment:
(1) Locations exposed to direct sunlight;
(2) Locations subject to sudden changes in environmental temperature;
(3) Dusty locations;
(4) Locations subject to vibration;
(5) Locations near heat generators;
(6) Locations with high humidity.
5. Turn ON the system only after the power has been turned OFF for more than 20
seconds. If the system is turned ON immediately after being turned OFF, the system
may not reboot properly and could malfunction.
6. Do not disconnect a transducer that remains in a live imaging state. This can
damage the system and / or transducer. Press [Freeze] key to freeze an image or
turn off the power of the system before connecting or disconnecting a transducer.
7. Remove ultrasound gel from the face of a transducer when the examination is
complete. Water in the gel may enter the acoustic lens and adversely affect or
damage the transducer array and lens.
8. You should properly back up the system to a secure external storage media,
including system configuration and settings and patient data. Data stored to the
system’s hard drive may be lost due to system failure, improper operation or
accident.
9. Do not apply external force to the control panel. The system may be damaged.
10. If the system is used in a small room, the room temperature may rise. Provide
proper ventilation and free air exchange.
11. To dispose of the system or any part, contact Mindray Customer Service Department
or sales representative. Mindray is not responsible for any system content or
accessories that have been discarded improperly.
12. To ensure optimal system operations, it is recommended that you maintain the
system under a Mindray service agreement. Various aspects of system performance
and operation can be maintained under the professional supervision of a service
representative.
13. Do not use gel, disinfectant, transducers or needle-guided brackets that are not
compatible with the system.
Safety Precautions IX

NOTE: 14. The replaceable fuse is inside the chassis. Refer replacing job to Mindray service
engineers or engineers authorized by Mindray only.
15. Do not turn OFF the power supply of the system during printing, file storage or
invoking other system operations. An interrupted process may not be completed,
and can become lost or corrupted.
16. If the system is powered off improperly during operation, it may result in data
damage or system failure.
17. Do not use a USB memory device (e.g., a USB flash drive, removable hard disk)
which has unsafe data. Otherwise system damage may result.
18. It is recommended to only use the video devices specified in this manual.
19. When copying files to USB storage device, do not pull out the USB storage device
forcibly, or damage to USB storage device or this system may occur.
20. Do not connect mobile hard disk with too many partitions.
21. When sending DICOM files or copying files from USB storage devices, do not press
the buttons on the control panel.
NOTE: The following definition of the WEEE label applies to EU member states
only: The use of this symbol indicates that this system should not be
treated as household waste. By ensuring that this system is disposed of
correctly, you will help prevent bringing potential negative consequences
to the environment and human health. For more detailed information with
regard to returning and recycling this system, please consult the
distributor from whom you purchased the system.
* For system products, this label may be attached to the main unit only.
Latex Alert
WARNING: Allergic reactions in latex (natural rubber) sensitive patients may range
from mild skin reactions (irritation) to fatal anaphylactic shock, and
may include difficulty in breathing (wheezing), dizziness, shock,
swelling of the face, hives, sneezing or itching of the eyes (FDA
Medical Alert on latex products, “Allergic Reactions to Latex-
containing Medical Devices”, issued on March 29, 1991).
When choosing a transducer sheath, it is recommended that you directly contact CIVCO for
obtaining transducer cover, pricing information, samples and local distribution information. For
CIVCO information, please contact the following:
CIVCO Medical Instruments
Tel: [phone]
WWW.civco.com
X Latex Alert

Warning Labels
The warning labels are attached to this system in order to call your attention to potential hazards.
The symbol on the warning labels indicates safety precautions. The warning labels use the
same signal words as those used in the operator’s manual.
Refer to the operator’s manual for detailed information about the warning labels. Read operator’s
manual carefully before using the system.
The name, pattern and meaning of each warning label are described as follows:
No. Label Meaning
1 Cautions against sitting on the system.
2
a) b)
a) Cautions that the system must not be used
around flammable gasses.
b) Urges Caution related to handling of the
transducers.
For handling of the transducers, refer to the
transducers’ operator’s manual.
3
a) b)
a) Cautions that the system must be placed
on a horizontal surface.
b) Cautions that the system must not be
removed covers because the high voltage
may cause electric shock.
Warning Labels XI